6-Fluoro-2-aminophenol

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Company Name: Liuyang huarui material technology co., ltd.  Gold
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Company Name: J & K SCIENTIFIC LTD.  
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Company Name: Jia Xing Isenchem Co.,Ltd  
Tel: 0573-85285100 18627885956
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6-Fluoro-2-aminophenol manufacturers

6-Fluoro-2-aminophenol Basic information
Product Name:6-Fluoro-2-aminophenol
Synonyms:6-Fluoro-2-Aminophenol;6-Fluoro-2-aminophen;3-Fluoro-2-hydroxyaniline 97%;2-Amino-6-fluorophenol97%;2-Amino-6-fluorophenol 97%;Phenol, 2-amino-6-fluoro-
CAS:53981-25-2
MF:C6H6FNO
MW:127.12
EINECS:
Product Categories:Aromatics;Metabolites & Impurities
Mol File:53981-25-2.mol
6-Fluoro-2-aminophenol Structure
6-Fluoro-2-aminophenol Chemical Properties
Boiling point 215.7±25.0 °C(Predicted)
density 1.347±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility DMSO (Slightly), Methanol (Slightly)
pka8.50±0.10(Predicted)
form Solid
AppearanceBrown to black Solid
InChIInChI=1S/C6H6FNO/c7-4-2-1-3-5(8)6(4)9/h1-3,9H,8H2
InChIKeyMDIAVSZFIQWYST-UHFFFAOYSA-N
SMILESC1(O)=C(F)C=CC=C1N
Safety Information
RIDADR 2811
HazardClass 6.1
PackingGroup 
HS Code 2921420090
MSDS Information
6-Fluoro-2-aminophenol Usage And Synthesis
Chemical PropertiesPurple crystals
UsesA metabolite of halogenated aniline.
Synthesis
2-Fluoro-6-nitrophenol

1526-17-6

6-Fluoro-2-aminophenol

53981-25-2

The general procedure for the synthesis of 6-fluoro-2-aminophenol from 2-fluoro-6-nitrophenol was as follows: 2-fluoro-6-nitrophenol (6.37 mmol, 1.00 g) was dissolved in methanol (100 mL), and 10% activated charcoal-loaded palladium catalyst (10% by weight of 2-fluoro-6-nitrophenol, 0.10 g) was added. The reaction system was displaced first with argon and then with hydrogen, each displacement lasting 15 min, during which magnetic stirring was maintained. Subsequently, the reaction was carried out at atmospheric pressure (using a hydrogen balloon) and under hydrogen atmosphere for 1 hour. Upon completion of the reaction, the gas in the reaction vessel was again replaced with argon for 15 minutes. The reaction mixture was filtered through a diatomaceous earth pad and washed with methanol (50 mL). The filtrate was concentrated under vacuum to give a red solid product. Purification by silica gel column chromatography (eluent ratio 1:1 hexane/chloroform) gave a white crystalline solid in 87% yield.

References[1] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 15, p. 3521 - 3525
[2] Patent: JP2016/124812, 2016, A. Location in patent: Paragraph 0115
[3] Patent: US2010/298334, 2010, A1. Location in patent: Page/Page column 46
[4] Patent: WO2005/118561, 2005, A1. Location in patent: Page/Page column 25
[5] Patent: US2005/124667, 2005, A1. Location in patent: Page/Page column 17
6-Fluoro-2-aminophenol Preparation Products And Raw materials
Raw materials2-Fluoro-6-nitrophenol-->Activated carbon-->Methanol-->Palladium-->Hydrogen
Preparation Products2-Chloro-7-fluorobenzo[d]oxazole
Tag:6-Fluoro-2-aminophenol(53981-25-2) Related Product Information
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